反应 #833551
ord-2012372a4ba14470831714445e2ab4ed
反应方程式
Na2CO3
4,6-Dimethyl-2-(2-oxo-ethylsulfanyl)nicotinonitrile
4-(2,3-dihydrobenzo[1,4]dioxin-5-yl)piperazine
sodium triacetoxyborohydride
→
2-{2-[4-(2,3-Dihydrobenzo[1,4]dioxin-5-yl)piperazin-1-yl]ethylsulfanyl}-6-methylnicotinonitrile
反应物
试剂
无
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1workup.ADDITIONadded until pH
- 2萃取The mixture was extracted with ethyl acetate
- 3其他the combined organic phases dried
- 4其他evaporated
- 5其他to give an oil which
- 6其他was subjected to purification by column chromatography (silica gel; ethyl acetate and heptane)
- 7其他giving an oil which
- 8其他precipitated as the oxalate salt (0.36 g) from acetone
- 9其他LC/MS (m/z) 397 (MH+), RT=1.91, purity: 97%
实验过程
4,6-Dimethyl-2-(2-oxo-ethylsulfanyl)nicotinonitrile (2.9 g) was dissolved in 1,2-dichloroethane (150 mL), a solution of 4-(2,3-dihydrobenzo[1,4]dioxin-5-yl)piperazine (2.6 g) in DMF (150 mL) was added, followed by addition of sodium triacetoxyborohydride (14.9 g) and stirring for 2 h. The mixture was poured on water and Na2CO3 added until pH reached 7-8. The mixture was extracted with ethyl acetate, the combined organic phases dried and evaporated to give an oil which was subjected to purification by column chromatography (silica gel; ethyl acetate and heptane) giving an oil which precipitated as the oxalate salt (0.36 g) from acetone. LC/MS (m/z) 397 (MH+), RT=1.91, purity: 97%.